Senior Incoming Quality Assurance (IQA) Supervisor (Granite City)

AbbVie in Granite City, IL

  • Type: Full Time
position filled
  • Supervise a team of technicians in the Quality function to include selection and hiring, setting performance expectations, performance assessment, train and staff development and resolution of personnel issues
  • Provide Quality support on the manufacturing shop floor
  • Responsible for supporting Operations efforts in meeting established production schedule
  • Partner with Operations employees to document exception documents, including re-inspection and resolve other outstanding plant quality/compliance issues
  • Propose changes update, author, and implement departmental procedures consistent with objectives of simplification and process efficiencies/improvements which ensure ongoing compliance
  • Provide leadership and act as primary resource at site
  • Investigate QC hold, quarantine and reject for materials not meeting standards, ensure the initiation of exception documentation and oversee the implementation of any corrective action
  • Responsible for the review and approval of Procedures and Change Requests
  • Assist/serve/provide feedback on continuous improvement initiatives/teams
  • Bachelor Degree, BA/BS in Science,Engineering, Business or related field or equivalent related experience required.
  • 2-3 years experience in QA, Manufacturing or Business teams. IQA experience is preferred.
  • Supervisory experience preferred.
  • Knowledge of regulations and standards affecting pharmaceutical products
  • Ability to partner with QA & Operations personnel in order to influence/make effective QA decisions that are consistent with regulatory requirements and support overall production demands
  • Ability to make effective QA decisions independently in a fast-paced production environment
  • Ability to independently manage QA team including hiring, coaching, counseling, and developing personnel with minimal support from QA management
  • Strong interpersonal and communication skills. Ability to effectively resolve conflict and lead efforts to resolve critical situations
  • Good writing skills to create, edit and review cGMP documents, operating procedures and manufacturing documents
  • Additional Information
  • Significant Work Activities and Conditions: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
  • Travel: No
  • Job Type: Experienced
  • Schedule: Full-time
  • Job Level Code: IC

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